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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1520827Generated: October 26, 2026

Boron tribromide → 3-methyl-4-(4-(trifluoromethyl)-1H-pyrazol-1-yl)phenol

https://huagongshe.com/reaction/1520827

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoron tribromideHCID 25134—
Reactant1-(4-methoxy-2-methylphenyl)-4-(trifluoromethyl)-1H-pyrazoleHCID 68156642—
SolventDichloromethaneHCID 6344—
Product3-methyl-4-(4-(trifluoromethyl)-1H-pyrazol-1-yl)phenolHCID 6531379899%

Reaction Steps

To a 0° C. solution of 1-(4-methoxy-2-methylphenyl)-4-(trifluoromethyl)-1H-pyrazole (400 mg, 2 mmol) in dichloromethane (5 mL) was added boron tribromide (1 g, 6 mmol). The mixture was allowed to warm to room temperature and stir overnight. The reaction was quenched with methanol (2 mL), diluted with water (10 mL), and extracted with dichloromethane (3×10 mL). The combined organics were dried over sodium sulfate, filtered, and concentrated to give 3-methyl-4-(4-(trifluoromethyl)-1H-pyrazol-1-yl)phenol (390 mg, 99%) as a brown solid. 1H NMR (400 MHz, CDCl3, δ): 7.83 (s, 1H), 7.74 (s, 1H), 7.08 (d, J=8.4 Hz, 1H), 6.65 (s, 1H), 6.62 (d, J=8.4 Hz, 1H), 5.57 (s, 1H), 2.05 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09073871B2
Source datasetuspto-grants-2015_07
ORD IDord-0d8173edd6d84316bef40f6f97292aeb
Source noteuspto-grants-2015_07